Spatially distinguished, multiplex nucleic acid analysis of biological specimens

Patent metadata

Field	Value
Publication number	US-11739372-B2
Application number	US-202318166853-A
Country	US
Kind code	B2
Filing date	Feb 9, 2023
Priority date	Apr 10, 2015
Publication date	Aug 29, 2023
Grant date	Aug 29, 2023

Abstract

A method for spatially tagging nucleic acids of a biological specimen, including steps of (a) providing a solid support comprising different nucleic acid probes that are randomly located on the solid support, wherein the different nucleic acid probes each includes a barcode sequence that differs from the barcode sequence of other randomly located probes on the solid support; (b) performing a nucleic acid detection reaction on the solid support to locate the barcode sequences on the solid support; (c) contacting a biological specimen with the solid support that has the randomly located probes; (d) hybridizing the randomly located probes to target nucleic acids from portions of the biological specimen; and (e) modifying the randomly located probes that are hybridized to the target nucleic acids, thereby producing modified probes that include the barcode sequences and a target specific modification, thereby spatially tagging the nucleic acids of the biological specimen.

First claim

The invention claimed is:

1. A method for spatially tagging target nucleic acids of a biological specimen, comprising:
(a) providing a solid support comprising a population of nucleic acid probes attached at randomly located positions on the solid support, wherein a nucleic acid probe in the population of nucleic acid probes comprises: (i) a target capture sequence and (ii) a spatial tag sequence that differs from spatial tag sequences of nucleic acid probes in the population at other randomly located positions on the solid support;
(b) performing a nucleic acid detection reaction to determine the spatial tag sequences at the randomly located positions on the solid support;
(c) contacting the biological specimen with a portion of the population of nucleic acid probes on the solid support;
(d) hybridizing one or more of the target capture sequences of the population of nucleic acid probes to target nucleic acids from the biological specimen that are proximal to the population of nucleic acid probes; and
(e) extending the one or more target capture sequences to produce extended probes that comprise complementary sequences to the target nucleic acids, or portions thereof, and the spatial tag sequences, thereby spatially tagging the target nucleic acids of the biological specimen.

2. The method of claim 1 , wherein step (a) further comprises amplifying the population of nucleic acid probes on the solid support, thereby producing nucleic acid clusters having copies of the spatial tag sequence and the target capture sequence at the randomly located positions on the solid support.

3. The method of claim 2 , wherein the nucleic acid clusters on the solid support have an average pitch of less than 10 microns and/or an average area of less than 100 microns.

4. The method of claim 1 , wherein the nucleic acid detection reaction is a sequencing reaction or a decoder probe hybridization reaction.

5. The method of claim 1 , wherein the solid support comprises an array of beads, where the population of nucleic acid probes are attached to beads in the array, wherein:
(i) step (a) comprises randomly distributing the beads on the solid support such that each bead in the array of beads occupies a randomly located position on the solid support; or
(ii) the solid support comprises wells having dimensions that accommodate no more than a single bead, wherein: the beads are attached to different spatial tag sequences and there a greater number of spatial tag sequences than number of wells, the solid support comprises at least 1×10 6 beads, the array of beads has an average pitch of less than 10 microns, and/or the beads have an average diameter of less than 10 microns.

6. The method of claim 1 , wherein the solid support comprises a pattern of discrete features.

7. The method of claim 2 , wherein the solid support comprises a gel coating, wherein a plurality of nucleic acid primers is attached to the gel coating, wherein a nucleic acid primer of the plurality of nucleic acid primers comprises a universal primer sequence that is common to the nucleic acid primers, and wherein a nucleic acid probe of the population of nucleic acid probes comprises a universal primer binding sequence that hybridizes to the universal primer sequence.

8. The method of claim 7 , wherein a second plurality of nucleic acid primers is further attached to the gel coating, wherein a nucleic acid primer of the second plurality of nucleic acid primers comprise a second universal primer sequence that is common to the nucleic acid primers of the second plurality of nucleic acid primers, and wherein the nucleic acid probe comprises a second universal primer binding sequence that hybridizes to the second universal primer sequence, and the amplifying comprises bridge amplification.

9. The method of claim 1 , wherein different nucleic acid probes of the population of nucleic acid probes hybridize to different target nucleic acids from the biological specimen.

10. The method of claim 1 , wherein different nucleic acid probes of the population of nucleic acid probes comprise a common target capture sequence, and the common target capture sequence comprises a poly(T) or a poly(A) sequence.

11. The method of claim 1 , wherein the method further comprises:
acquiring an image of the biological specimen in contact with the solid support; and correlating the determined spatial tag sequences at the randomly located positions on the solid support with location in the image of the biological specimen.

12. The method of claim 1 , wherein the method further comprises:
removing the extended probes from the solid support; and
determining the sequences of the target nucleic acids, or portions thereof, and the spatial tag sequences for the extended probes that have been removed from the solid support.

13. The method of claim 12 , wherein determining the sequences of the target nucleic acids, or portions thereof, and the spatial tag sequences for the extended probes that have been removed from the solid support comprises sequencing-by-synthesis, sequencing-by-hybridization, or sequencing-by-ligation.

14. The method of claim 1 , wherein the method further comprises:
removing the extended probes from the solid support; and
attaching the extended probes that have been removed from the solid support to a second solid support.

15. The method of claim 14 , wherein the second solid support comprises a flowcell.

16. The method of claim 1 , further comprising amplifying the extended probes and the spatial tag sequence or a complement thereof, thereby generating amplification products comprising target nucleic acids or complements thereof or a portion of the target nucleic acids or complements thereof, and the spatial tag or a complement thereof.

17. The method of claim 16 , wherein the amplifying is selected from the group consisting of: polymerase chain reaction, rolling circle amplification, multiple strand displacement amplification, and random prime amplification.

18. The method of claim 16 , wherein the method further comprises performing a sequencing reaction on the amplification products to determine all or a portion of the target nucleic acid sequences or complements thereof, and the spatial tag sequences or complements thereof, thereby determining a spatial location of target nucleic acids in the biological specimen, wherein the sequencing reaction comprises sequencing-by-synthesis, sequencing-by-hybridization, or sequencing-by-ligation.

19. The method of claim 18 , wherein determining the spatial location of target nucleic acids in the biological specimen further comprises correlating the determined sequences of the target nucleic acids or complements thereof and the spatial tag sequences or complements thereof with an acquired image of the biological specimen, wherein the acquired image was previously correlated with the randomly located spatial tag sequences on the solid support.

20. The method of claim 16 , wherein the method further comprises removing the amplification products from the solid support and, pooling the amplification products to form a mixture of amplification products that have been removed from the solid support, and attaching the amplification products that have been removed from the solid support to a second solid support.

21. The method of claim 1 , wherein the solid support was located in or on a flowcell during step (b), and the solid support is removed from the flow cell during step (c) or the flowcell is opened to expose the solid support dur

Assignees

• Spatial Transcriptomics Ab
• Illumina Inc

Inventors

• Frisen Jonas
• Stahl Patrik
• Lundeberg Joakim
• Cann Gordon M
• Bazargan Leila
• Aravanis Alex

Classifications

• B01L3/502

  with fluid transport, e.g. in multi-compartment structures · CPC title

• B01L3/5055

  Hinged, e.g. opposable surfaces · CPC title

• B01L2300/0877

  Flow chambers · CPC title

• B01L2300/163

  Biocompatibility · CPC title

• C12Q1/6834 Primary

  Enzymatic or biochemical coupling of nucleic acids to a solid phase · CPC title